Daito Pharmaceutical Co., Ltd.
FDA inspection history in Toyama-City, Japan, 2017 to 2023
- 4
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2020: one Form 483; 2022: one Form 483; 2023: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at Toyama-City, Japan.
- 2020–23Three Form 483s, at Toyama-City, Japan.
- 2020The longest 483 on file: 10 observations over 3 pages at Toyama-City, Japan.
Cited most
Across all Daito Pharmaceutical Co. observations on file
- 21 CFR 211.22Responsibilities of quality control unit6
- 21 CFR 211.68Automatic, mechanical, and electronic equipment4
- 21 CFR 211.192Production record review3
- 21 CFR 211.160General requirements2
- 21 CFR 211.194Laboratory records2
The complete Daito Pharmaceutical Co. file.
All 4 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Toyama-City, Japan
Four Form 483s · 2017 to 2023 · 22 observations
Latest: Form 483, Dec 19, 2023 →
Documents
4 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2023-12-19 | 483 Form 483 | Toyama-City, Japan | 2 | $99 |
| 2022-09-16 | 483 Form 483 | Toyama-City, Japan | 2 | $99 |
| 2020-01-31 | 483 Form 483 | Toyama-City, Japan | 10 | $99 |
| 2017-11-10 | 483 Form 483 | Toyama-City, Japan | 8 | $99 |
Investigators on these documents
Arsen Karapetyan (1)Cheryl Clausen (1)Santiago Gallardo Johnson (1)Truong X. Nguyen (1)
FEI number 3002806779 · most recent document Dec 19, 2023
About Daito Pharmaceutical Co., Ltd.
How many FDA Form 483s has Daito Pharmaceutical Co., Ltd. received?
FDA Intel has 4 Form 483s on file for Daito Pharmaceutical Co., Ltd.; the most recent is dated Dec 19, 2023.
When was Daito Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Daito Pharmaceutical Co., Ltd. is a Form 483 dated Dec 19, 2023, for the site in Toyama-City, Japan.
What did FDA cite at Daito Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Daito Pharmaceutical Co., Ltd. are 21 CFR 211.22 (Responsibilities of quality control unit), 6 times; 21 CFR 211.68 (Automatic, mechanical, and electronic equipment), 4 times; 21 CFR 211.192 (Production record review), 3 times.